Article | April 22, 2020

Protocol Feasibility To Promote Trial Efficiency

Source: Advarra

By Dr. Wendy Tate, Director, Research Operations, Forte

 Choosing The Right Solution: Improving the Clinical Trial Site Feasibility Process

Scientific abstracts and articles have reported that 20-50% of studies do not accrue subjects at the site level (1-6). This contributes to a significant amount of waste in clinical research, particularly in the forms of staff time and monetary resources. Such waste can be reduced through the careful selection of clinical trials to activate early in the process, before investing a lot of resources. The protocol feasibility review process achieves this by providing a method to review the logistical aspects of a clinical trial prior to starting the activation process.

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